You have changed your country from  to  . Please be aware that this will change the currency in the purchasing process.

Reassurance, Refunds & Replacements

If your product does not perform as described on this datasheet, we will refund or replace your product...

Read our guarantee »
 

Anti-LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339)

CodeSizePriceAbpointsAvailability
    
 
  • -
  •   
  •   
  •   
  •  
  •   
  •   
Updating...

Overview

Product name

Anti-LAMP2 antibody [ABL-93] - Lysosome Marker
See all LAMP2 products (21) ...

Description

Rat monoclonal [ABL-93] to LAMP2 - Lysosome Marker

Tested applications

Flow Cyt, IHC-Fr, IPmore details

Cross reactivity

Reacts with

Mouse

Immunogen

Glycoproteins purified from BALB/c embryo 3T3 cell line (Mouse)

Properties

Form

Liquid

Storage instructions

Shipped at 4°C. Upon delivery aliquot and store at -20°C or -80°C. Avoid repeated freeze / thaw cycles.

Storage buffer

Preservative: None
Constituents: 100mM Borate buffered saline, pH 8.2

Concentration

Concentration information loading...

Purity

IgG fraction

Clonality

Monoclonal

Clone number

ABL-93

Isotype

IgG2a

Light chain type

kappa

  • Immunohistochemistry (Frozen sections) - LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339)Immunohistochemistry (Frozen sections) - LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339) image (enlarge)

  • Flow Cytometry-LAMP2 antibody [ABL-93] - Lysosome Marker(ab25339)Flow Cytometry-LAMP2 antibody [ABL-93] - Lysosome Marker(ab25339) image (enlarge)

Applications

Show applications key

Our Abpromise guarantee covers the use of ab25339 in the following tested applications.

The application notes include recommended starting dilutions; optimal dilutions/concentrations should be determined by the end user.

Target

Function

Implicated in tumor cell metastasis. May function in protection of the lysosomal membrane from autodigestion, maintenance of the acidic environment of the lysosome, adhesion when expressed on the cell surface (plasma membrane), and inter-and intracellular signal transduction. Protects cells from the toxic effects of methylating mutagens.

Tissue specificity

Isoform LAMP-2A is highly expressed in placenta, lung and liver, less in kidney and pancreas, low in brain and skeletal muscle. Isoform LAMP-2B is highly expressed in skeletal muscle, less in brain, placenta, lung, kidney and pancreas, very low in liver.

Involvement in disease

Defects in LAMP2 are the cause of Danon disease (DAND) [MIM:300257]; also known as glycogen storage disease type 2B (GSD2B). DAND is a lysosomal glycogen storage disease characterized by the clinical triad of cardiomyopathy, vacuolar myopathy and mental retardation. It is often associated with an accumulation of glycogen in muscle and lysosomes.

Sequence similarities

Belongs to the LAMP family.

Post-translational
modifications

O- and N-glycosylated; some of the 16 N-linked glycans are polylactosaminoglycans.

Cellular localization

Cell membrane. Endosome membrane. Lysosome membrane. This protein shuttles between lysosomes, endosomes, and the plasma membrane.

Target information above from: UniProt accessionP13473 The UniProt Consortium
The Universal Protein Resource (UniProt) in 2010
Nucleic Acids Res. 38:D142-D148 (2010).

Information by UniProt

Alternative names

  • CD107 antigen-like family member B antibody
  • CD107b antibody
  • CD107b antigen antibody
  • Igp110 antibody
  • Igp2 antibody
  • LAMP 2 antibody
  • LAMP 2C antibody
  • LAMP B antibody
  • LAMP-2 antibody
  • LAMP2 antibody
  • LAMP2_HUMAN antibody
  • LAMPB antibody
  • LGP110 antibody
  • Lysosomal associated membrane protein 2C antibody
  • Lysosome associated membrane glycoprotein 2 precursor antibody
  • Lysosome associated membrane protein 2 antibody
  • Lysosome-associated membrane glycoprotein 2 antibody
  • Lysosome-associated membrane protein 2 antibody
  • MAC3 antibody
see all

Database links

Anti-LAMP2 antibody [ABL-93] - Lysosome Marker images:

  Immunohistochemistry (Frozen sections) - LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339)

Immunohistochemistry (Frozen sections) - LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339)

ab25339 staining LAMP2 from mouse liver cells by Immunohistochemistry (Frozen sections). The fresh tissue was cut into small pieces, put into OCT, and frozen in liquid nitrogen. 5µm sections were prepared using a cyrostat. The tissue section was fixed in 5% paraformaldehyde and blocked in 5% serum with 0.05% saponin to increase the permeability. The sample was incubated with ab25339 (1/100 dilution) overnight, and incubated with secondary antibody (Cy2 conjugated donkey anti-rat IgG) for 2 hours. After staining with DAPI (1/1000 dilution) for 2 minutess, the section was mounted.

This image is courtesy of an anonymous Abreview

See Abreview

  Flow Cytometry-LAMP2 antibody [ABL-93] - Lysosome Marker(ab25339)

Flow Cytometry-LAMP2 antibody [ABL-93] - Lysosome Marker(ab25339)

Overlay histogram showing RAW 264.7 cells stained with ab25339 (red line). The cells were fixed with 4% paraformaldehyde (10 min) and then permeabilized with 0.1% PBS-Tween for 20 min. The cells were then incubated in 1x PBS / 10% normal goat serum / 0.3M glycine to block non-specific protein-protein interactions followed by the antibody (ab25339, 1µg/1x106 cells) for 30 min at 22°C. The secondary antibody used was DyLight® 488 goat anti-rat IgG (H+L) (ab98386) at 1/500 dilution for 30 min at 22°C. Isotype control antibody (black line) was rat IgG2a, kappa monoclonal [aRTK2758] (ab18450, 2µg/1x106 cells) used under the same conditions. Acquisition of >5,000 events was performed. This antibody gave a positive signal in RAW 264.7 cells fixed with 80% methanol/permeabilized in 0.1% PBS-Tween used under the same conditions.

References for Anti-LAMP2 antibody [ABL-93] - Lysosome Marker (ab25339)

This product has been referenced in:

  • Sun Yet al. Neuronopathic Gaucher disease in the mouse: viable combined selective saposin C deficiency and mutant glucocerebrosidase (V394L) mice with glucosylsphingosine and glucosylceramide accumulation and progressive neurological deficits. Hum Mol Genet 19:1088-97 (2010). IHC-Fr; Mouse.Read more (PubMed: 20047948) »
  • Cardone Met al. Correction of Hunter syndrome in the MPSII mouse model by AAV2/8-mediated gene delivery. Hum Mol Genet 15:1225-36 (2006). IHC-Fr; Mouse.Read more (PubMed: 16505002) »

See all 5 publications for this product

Publishing research using ab25339? Please let us know so that we can cite the reference in this datasheet

Please note: All products are "FOR RESEARCH USE ONLY AND ARE NOT INTENDED FOR DIAGNOSTIC OR THERAPEUTIC USE"